Variant #0001075727 (NC_000001.10:g.145507646G>A, NM_005105.3:c.-21G>A (RBM8A))

Chromosome 1
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.145507646G>A
DNA change (hg38) -
Published as -
ISCN -
DB-ID RBM8A_000002 See all 79 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs139428292
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.0183 View details
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2026-04-30 11:03:01 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RBM8A NM_005105.3 +/. - c.-21G>A r.(?) p.(?)


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